In re Ryan

480 F.2d 1388, 178 U.S.P.Q. (BNA) 480, 1973 CCPA LEXIS 304
CourtCourt of Customs and Patent Appeals
DecidedJuly 19, 1973
DocketPat. Appeal No. 8982
StatusPublished

This text of 480 F.2d 1388 (In re Ryan) is published on Counsel Stack Legal Research, covering Court of Customs and Patent Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Ryan, 480 F.2d 1388, 178 U.S.P.Q. (BNA) 480, 1973 CCPA LEXIS 304 (ccpa 1973).

Opinion

LANE, Judge.

This appeal is from the decision of the Patent Office Board of Appeals sustaining the § 103 rejection of claims 1, 2, 3 and 5 of appellant’s application Serial No. 673,111 filed October 5, 1967. The board concluded that the subject matter would have been obvious to one of ordinary skill in the art in light of the state of the art admitted by appellant. No references were cited. We affirm the board’s decision.

The claims are directed to an improvement in the method of continuously regenerating exhausted cationic ion exchange resin particles. Using the purification of water as an example of a cationic ion exchange process, undesired ions, such as calcium and magnesium, are removed by contact with a resin which gives up more desirable ions, such as hydrogen ions, in exchange for the undesired ions. After a time, the resin must itself be regenerated by replacement of the captured ions with new hydrogen ions. Once regenerated, the ion exchange resin may be washed and returned to service. On a practical, commercial level, the initial exchange, regeneration of the resin, washing of the regenerated resin, and return of the washed, regenerated resin to ion exchange service are carried out continuously.

As described in appellant’s specification and brief on appeal, it was known prior to appellant’s invention to use a regeneration column in which exhausted resin particles were introduced near the top of the column and carried downward while regenerant solution, such as sulfuric acid or hydrochloric acid, was countercurrently passed through the column. The chemical process occurring in such a situation was the exchange of hydrogen ions coming from the acid for the mineral ions, such as calcium or magnesium, picked up by the resin during the previous ion exchange step. The continuous downward flow of resin in the regeneration column was accomplished by the recirculation of previously used regenerant solution. The specification more particularly describes the prior practice as follows:

In charging the column with exhausted resin particles from the reservoir, a piston-type action is employed whereby the non-turbulent, downward flow of liquid within the column allows exhausted resin particles to flow down into the column. Prior to the present invention, such downward flow was created by depressurizing the column and withdrawing liquid from a lower portion while allowing the re-introduction of exhausted regenerant near the top. The exhausted regenerant was introduced from a surge tank which retained a sufficient volume before disposing of it in the waste drain. While such a procedure is satisfactory for most combinations of resin and regenerant, severe difficulties are encountered where a relatively insoluble material is formed [1390]*1390during the regeneration process. Commonly, such a material is formed where sulfuric acid is employed to regenerate hydrogen-form strong acid cation exchange resin particles. The exhausted resin retains calcium ions, removed from the raw water in the service column, which are exchanged for hydrogen ions in the sulfuric acid, forming a supersaturated solution of calcium sulfate. Holding the exhausted regenerant in a surge tank, and agitating it by re-introducing it into the column, encourages precipitation of the calcium sulfate. The introduction of seed crystals into the column causes further precipitation, agglomerating with the resin particles and eventually, plugging the column. The precipitate may also plug the filter used at the regenerant outlet, interfering with the movement of regenerant.
Because of the problem of calcium sulfate precipitation, it has been considered difficult to employ sulfuric acid in the countercurrent regeneration of hydrogen-form cationic ion exchange resins. Instead, hydrochloric acid has been used. Although the use of hydrochloric acid avoids the precipitation of insoluble materials, it is much more expensive and therefore less desirable than sulfuric acid.

Appellant overcomes the problems theretofore encountered by replacing the previously used regenerant solution which carries the resin through the column with a liquid described generically in the specification as follows:

[I] t must be free of insoluble materials that could cause precipitation within the column, as well as materials that would react within the column to form a precipitate. Normally the second liquid will be water or water containing an additive to inhibit precipitation.

That modification of the prior art process enables the use of the less expensive sulfuric acid. In the claims, the liquid is limited to water.

Claim 1 reads as follows:
1. In the continuous regeneration of cationic ion exchange resin particles with sulfuric acid in a column normally regenerating said particles by an upward flow of regenerant between regenerant inlet and outlet means wherein exhausted resin particles are periodically introduced into an upper portion of said column and liquid is simultaneously removed at a drain point, the improvement comprising introducing water into said column at a point above said drain point during the introduction of said exhausted resin particles and at a rate sufficient to maintain said column filled with material, said water being free of insoluble materials that could cease [cause?] precipitation within said column, and said water also being free from materials that can react within said column to form a precipitate. [Emphasis added.]

Dependent claims 2, 3 and 5 impose limitations which appellant does not separately argue.

The Examiner’s Answer states as follows :

In the original specification, in each amendment, and in the Brief, applicant has acknowledged that the continuous countercurrent ion exchange system generally is known and that an auxiliary liquid is used to assure smooth resin transfer to the regenerating column in such systems. It is further acknowledged that the cause of clogging which has been experienced as a problem in such systems when sulfuric acid regenerant is used was known to be the precipitation of insoluble sulfates, particularly calcium sulfate.
* * * [Appellant’s discovery was] that precipitation of calcium sul[1391]*1391fate in the regeneration column is less likely to occur if water is substituted for the acidic calcium sulfate solution in the procedure described above. It is the examiner’s position that this “discovery” is at once obvious to one of ordinary skill in the art of chemistry. That is to say, the solution to the problem is plain upon the face of the description of the problem. [Emphasis added.]

The board generally agreed with the examiner, holding as follows:

The alleged invention lies in the utilization of water in a cation ion exchange process whereby undesirable precipitates are eliminated by introducing water into the column at the time the liquid from a surge tank is being drained off. Appellant’s main contention is that he discovered the source of the problem, i.e., precipitation occurring in the surge tank, and then solved the problem, i.e., the avoidance of reintroducing the contents of the surge tank back into the column. Instead, water is introduced above the drain point. It would appear to be obvious that any liquid containing spent sulfuric acid regenerant would contain sulfate precipitates.

Free access — add to your briefcase to read the full text and ask questions with AI

Cite This Page — Counsel Stack

Bluebook (online)
480 F.2d 1388, 178 U.S.P.Q. (BNA) 480, 1973 CCPA LEXIS 304, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-ryan-ccpa-1973.